Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo.
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Adeno-associated virus vector integrationAdeno-associated Virus as a Mammalian DNA VectorNeuroanatomy goes viral!Adeno-associated virus: from defective virus to effective vectorSelf-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesisGenetic fate of recombinant adeno-associated virus vector genomes in muscleAAV recombineering with single strand oligonucleotides.Distributed probing of chromatin structure in vivo reveals pervasive chromatin accessibility for expressed and non-expressed genes during tissue differentiation in C. elegans.Large-scale molecular characterization of adeno-associated virus vector integration in mouse liver.Evaluation of a rapamycin-regulated serotype 2 adeno-associated viral vector in macaque parotid glandsCharacterization of Fabry mice treated with recombinant adeno-associated virus 2/8-mediated gene transfer.Extrachromosomal recombinant adeno-associated virus vector genomes are primarily responsible for stable liver transduction in vivo.A NEW RECOMBINANT ADENO-ASSOCIATED VIRUS (AAV)-BASED RANDOM PEPTIDE DISPLAY LIBRARY SYSTEM: INFECTION-DEFECTIVE AAV1.9-3 AS A NOVEL DETARGETED PLATFORM FOR VECTOR EVOLUTION.Large-scale analysis of adeno-associated virus vector integration sites in normal human cells.Directed evolution of novel adeno-associated viruses for therapeutic gene delivery.Chromosomal integration and homologous gene targeting by replication-incompetent vectors based on the autonomous parvovirus minute virus of mice.Liver transduction with recombinant adeno-associated virus is primarily restricted by capsid serotype not vector genotype.Scalable generation of high-titer recombinant adeno-associated virus type 5 in insect cells.A limited number of transducible hepatocytes restricts a wide-range linear vector dose response in recombinant adeno-associated virus-mediated liver transductionCardiac gene therapyAdeno-associated viral vector-mediated gene transfer results in long-term enzymatic and functional correction in multiple organs of Fabry mice.Gene replacement therapies for duchenne muscular dystrophy using adeno-associated viral vectors.Parvovirus-mediated gene transfer for the haemophilias.Consequences of DNA-dependent protein kinase catalytic subunit deficiency on recombinant adeno-associated virus genome circularization and heterodimerization in muscle tissue.Hybrid adeno-associated viral vectors utilizing transposase-mediated somatic integration for stable transgene expression in human cells.Adeno-associated viruses undergo substantial evolution in primates during natural infections.Assessment of the safety and biodistribution of a regulated AAV2 gene transfer vector after delivery to murine submandibular glandsSafety of adeno-associated virus gene therapy vectors: a current evaluation.Perinatal gene transfer to the liver.Native molecular state of adeno-associated viral vectors revealed by single-molecule sequencingExistence of transient functional double-stranded DNA intermediates during recombinant AAV transductionSelf-Complementary Adeno-Associated Virus Vectors Improve Transduction Efficiency of Corneal Endothelial Cells.Integration frequency and intermolecular recombination of rAAV vectors in non-human primate skeletal muscle and liver.Genome-wide RNAi screening identifies host restriction factors critical for in vivo AAV transductionStability and Safety of an AAV Vector for Treating RPGR-ORF15 X-Linked Retinitis Pigmentosa.DNA palindromes with a modest arm length of greater, similar 20 base pairs are a significant target for recombinant adeno-associated virus vector integration in the liver, muscles, and heart in mice.The role of DNA-PKcs and artemis in opening viral DNA hairpin termini in various tissues in mice.AAV vectors containing rDNA homology display increased chromosomal integration and transgene persistence.AAV vectors for the nucleolusPrecise hit: adeno-associated virus in gene targeting.
P2860
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P2860
Recruitment of single-stranded recombinant adeno-associated virus vector genomes and intermolecular recombination are responsible for stable transduction of liver in vivo.
description
2000 nî lūn-bûn
@nan
2000 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2000年の論文
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2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
name
Recruitment of single-stranded ...... transduction of liver in vivo.
@ast
Recruitment of single-stranded ...... transduction of liver in vivo.
@en
type
label
Recruitment of single-stranded ...... transduction of liver in vivo.
@ast
Recruitment of single-stranded ...... transduction of liver in vivo.
@en
prefLabel
Recruitment of single-stranded ...... transduction of liver in vivo.
@ast
Recruitment of single-stranded ...... transduction of liver in vivo.
@en
P2093
P2860
P1433
P1476
Recruitment of single-stranded ...... transduction of liver in vivo.
@en
P2093
P2860
P304
P356
10.1128/JVI.74.20.9451-9463.2000
P577
2000-10-01T00:00:00Z